metformin hydrochloride

Generic: metformin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7534
Product ID 50090-7534_c139747e-272f-417b-89a4-89121d5c0533
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217631
Listing Expiration 2026-12-31
Marketing Start 2023-10-06

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907534
Hyphenated Format 50090-7534

Supplemental Identifiers

RxCUI
860981
UNII
786Z46389E

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metformin hydrochloride (source: ndc)
Generic Name metformin hydrochloride (source: ndc)
Application Number ANDA217631 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7534-0)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7534-1)
source: ndc

Packages (2)

50090-7534-0 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7534-0) 50090-7534-1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7534-1)

Ingredients (1)

metformin hydrochloride (750 mg/1)

Linked Drug Pages (1)

METFORMIN HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c139747e-272f-417b-89a4-89121d5c0533", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["c0ff557c-fa50-46f6-aa77-36a4df354e80"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7534-0)", "package_ndc": "50090-7534-0", "marketing_start_date": "20250408"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7534-1)", "package_ndc": "50090-7534-1", "marketing_start_date": "20250408"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7534_c139747e-272f-417b-89a4-89121d5c0533", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7534", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20231006", "listing_expiration_date": "20261231"}